Exchange-correlation energy in molecules: A variational quantum Monte Carlo study

Journal Article · Fri Sep 15 00:00:00 EDT 2006 · Physical Review. A

DOI:https://doi.org/10.1103/PHYSREVA.74.032507· OSTI ID:20857695

Hsing, C R ^[1]; Chou, M Y ^[2]; Lee, T K ^[1]

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1. Institute of Physics, Academia Sinica, Nankang, Taipei, Taiwan 11529 (China)
2. School of Physics, Georgia Institute of Technology, Atlanta, Georgia 30332-0430 (United States)

We have used the combination of the coupling-constant integration procedure and the variational quantum Monte Carlo method to study the exchange-correlation (XC) interaction in small molecules: Si{sub 2}, C{sub 2}H{sub 2}, C{sub 2}H{sub 4}, and C{sub 2}H{sub 6}. In this paper we report the calculated XC energy density, a central quantity in density functional theory, as deduced from the interaction between the electron and its XC hole integrated over the interaction strength. Comparing these 'exact' XC energy densities with results using the local-density approximation (LDA), one can analyze the errors in this widely used approximation. Since the XC energy is an integrated quantity, error cancellation among the XC energy density in different regions is possible. Indeed we find a general error cancellation between the high-density and low-density regions. Moreover, the error distribution of the exchange contribution is out of phase with the error distribution of the correlation contribution. Similar to what is found for bulk silicon and an isolated silicon atom, the spatial variation of the errors of the LDA XC energy density in these molecules largely follows the sign and shape of the Laplacian of the electron density. Some noticeable deviations are found in Si{sub 2} in which the Laplacian peaks between the atoms, while the LDA error peaks in the regions 'behind' atoms where a good portion of the charge density originates from an occupied 1{sigma}{sub u} antibonding orbital. Our results indicate that, although the functional form could be quite complex, an XC energy functional containing the Laplacian of the energy is a promising possibility for improving LDA.

• OSTI ID: 20857695
• Journal Information: Physical Review. A, Vol. 74, Issue 3; Other Information: DOI: 10.1103/PhysRevA.74.032507; (c) 2006 The American Physical Society; Country of input: International Atomic Energy Agency (IAEA); ISSN 1050-2947
• Country of Publication: United States
• Language: English

Related Subjects

74 ATOMIC AND MOLECULAR PHYSICS
ACETYLENE
APPROXIMATIONS
ATOMS
CHARGE DENSITY
CHEMICAL BONDS
COUPLING CONSTANTS
DENSITY FUNCTIONAL METHOD
DISTRIBUTION
ELECTRON CORRELATION
ELECTRON DENSITY
ELECTRONS
ENERGY DENSITY
ERRORS
ETHANE
ETHYLENE
HOLES
LAPLACIAN
MOLECULES
MONTE CARLO METHOD
SILICON
VARIATIONS